Research – TherapeuticsMD (TXMD) – First quarter 2019 earnings update

Tuesday, May 7, 2019

TherapeuticsMD (TXMD)

Will Revenue Trends From Imvexxy be Recognized?

TherapeuticsMD Inc is a major drug manufacturing with a focus on creating and commercializing products targeted exclusively for women. The company intends to commercialize advanced hormone therapy pharmaceutical products. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Solid Imvexxy
    Revenue Growth. 
    Net revenue generated by Imvexxy reached $2.0 million in Q1 2019 (+122%) compared to $0.9 in the fourth quarter of 2018 with sustained growth in prescription and refill rates; approximately 31,200 prescriptions in April 2019 (47,500 prescriptions in Q4 2018). In our view, increasing market share of Imvexxy will be meaningful to eradicate skepticism on commercialization.
  • Bijuva Launch to Follow
    with Annovera. 
    Annovera is set to launch in Q3 2019, following Bijuva’s launch in April 2019. We continue to highlight the market and cost synergies of Bijuva and Imvexxy, and also no…






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Research – Dyadic (DYAI) – Expanding partnership portfolio

Tuesday, April 30, 2019

Dyadic International (DYAI)

Sub-Licensing Agreement Providing Optionality for C1 Technology.

Dyadic International Inc. is a biotechnology company developing a proprietary C1 expression platform to express and manufacture biologic products. The C1 technology is part of a fungi expression system, which utilizes inexpensive substrates yielding a high level of production. Dyadic is currently improving and optimizing the production of biological products in a C1 expression system.

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 

  • Announces significant licensing agreement. Australian based drug development and contract
    manufacturing firm, Luina Bio, announced plans to utilize Dyadic’s C1 gene
    expression technology platform for the development and commercialization of
    biological products to prevent and treat animal diseases. This is the company’s
    first sub-licensing agreement, which, we believe, validates the company’s
    proprietary C1 technology.
  • Impressive list of partners. Luina Bio is the first licensing move for the company’s
    technology and adds to a list of significant R&D partnerships with
    pharmac…


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Research – TherapeuticsMD (TXMD) – Assumption of Coverage

Monday, April 29, 2019

TherapeuticsMD (TXMD)

Can the Early Commercial Success Eradicate the Stock Overhang?

TherapeuticsMD Inc is a major drug manufacturing with a focus on creating and commercializing products targeted exclusively for women. The company intends to commercialize advanced hormone therapy pharmaceutical products. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 

  • Assumption of Coverage with Outperform Rating and $13 Price
    Target. 
    We are assuming coverage of TherapeuticsMD with an Outperform rating and Price Target of $13, based on an NPV analysis of the
    pipeline. Three product approvals were granted by the FDA in 2018 providing a
    solid foundation for the company to become a significant player in the
    women’s health space.
  • Strong Player in Women’s Health. Three product approvals granted in 2018 include; i) Imvexxy
    for patients with vulvovaginal atrophy (VVA), ii) Bijuva (estradiol and
    progesterone) to treat vasomot…





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NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
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Research – Genprex (GNPX) – Initiation of Coverage

Friday, April 26, 2019

Genprex (GNPX)

Poised to Emerge as a Leader in Cancer Gene Therapy.

Genprex Inc is a US-based clinical stage gene therapy company. It is engaged in developing a new approach to treating cancer, based upon its novel proprietary technology platform, including initial product candidate, Oncoprex immunogene therapy.

Cosme Ordoñez, M.D., Ph. D. , Life Sciences Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 

  • Coverage
    Initiation
    . We are initiating coverage of Genprex, Inc. with an
    Outperform Rating and a 
    $5.00 target price.
  • Unique Gene
    Therapy Technology
    . We believe that Genprex will emerge as a leader in the area
    of gene therapy for the treatment of cancer. The Company is developing a unique
    platform technology consisting on the use of lipid nano…





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NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
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IPO Podcast Series: Drug Disruption

Episode Two: Drug Disruption

In the second episode of the IPO podcast series, Brant Pinvidic (host of the iTunes top-trending Hollywood podcast “Why I’m Not…”) probes into the positive aspects of being “disruptive.” Changing what is viewed as the norm – disrupting the status quo -can result in very positive change… Like Uber and Airbnb. Here Brant looks for disruption in healthcare; ways to reduce the costs associated with prescription drugs. He interviews the CEO of Dyadic International who believes his company has the answer. You be the judge.

The most innovative Ideas, the inspirational People behind them, and the wealth of Opportunities they create… that’s IPO from Channelchek.

watch the IPO series trailer

Research – Dyadic (DYAI) – Nasdaq Up-Listing Approved

Monday, April 15, 2019

Dyadic International (DYAI)

The Importance Behind The Nasdaq Up-Listing.

Dyadic International Inc. is a biotechnology company developing a proprietary expression platform to manufacture of biologic products. The company is employing C1 technology, part of a fungi expression system, to produce variety of modalities of biologic products, including vaccines, oncolytic viruses, monoclonal and bispecific antibodies, as well as biosimilars. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 

  • Important Milestone Accomplishment. Dyadic has announced the up-listing of its common stock on The Nasdaq
    Capital Market Exchange under stock symbol “DYAI”. The company has
    maintained the stock price requirement, for Nasdaq, following its SEC filing on
    February 2019. Trading will commence as early as 

    April 17, 2019. We believe this
    is an important milestone for the company and its current and future investors. 
  • Why is this important?  The company has accomplished key
    milestones as guided, including the SEC filing and the Nasdaq up-listing. The
    stock has gained +112% YTD 2019. We believe the biggest potential benefit from
    the up-listing is increased visibility and tran…





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Research – Trovagene (TROV) – Updated prostate cancer data

Wednesday, April 3, 2019

Trovagene Inc. (TROV)

Updated early prostate cancer data demonstrates sustained PSA levels.

TrovaGene Inc is a US-based life science company which focuses on the development and commercialization of a proprietary molecular genetic detection technology for use in pharmaceutical development, clinical research and medical testing across a variety of clinical disciplines, including oncology and virology. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 

  • AACR
    Presentation. 
    The company had the second presentation from a Phase 2 study
    of onvansertib in combination with Zytiga/prednisone in patients with metastatic
    castration-resistant prostate cancer (mCRPC), at the American Association for
    Cancer Research (AACR) annual meeting today, following the update from the
    acute myeloid leukemia (AML) trial (refer to the note published on April 2nd,
    2019).
  • Data Update in
    Prostate Cancer.  
    Onvansertib in combination with Zytiga/prednisone treatment
    achieved a reduction of prostate specific antigen (PSA) levels in 2 out of
    6 mCRPC patients. The previous data reported at
    the Genitourinary Cancers Symposium (ASCO-GU, on February) showed
    reduced PSA levels, however levels were relapsed. The company plans to
    comm
    … 







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Research – Trovagene (TROV) – Update on data readout

Tuesday, April 2, 2019

Trovagene Inc. (TROV)

Improved and updated data from AML patients.

TrovaGene Inc is a US-based life science company which focuses on the development and commercialization of a proprietary molecular genetic detection technology for use in pharmaceutical development, clinical research and medical testing across a variety of clinical disciplines, including oncology and virology. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.  

  • AACR Data
    Presentation.  
    The company presented data from a Phase 1b clinical trial of
    onvansertib in patients with acute myeloid leukemia (AML) at the American
    Association for Cancer Research (AACR) annual meeting on April 1st, 2019. The
    anti-leukemic activity improved with an increased number of patients treated.
    The disease control rate (DCR) rose to 89% (17/19 patients) from previous
    reported rate of 83% (10/12 patients) at The American Society of
    Hematology (ASH) on December 2018.
  • Digging Through Data. In addition to the improved DCR,  the overall response
    rate also increased; one patient with complete response (CR), one
    incomplete blood recovery (iCR), one morphologic leukemia-freestate (MLFS) and
    one partial response (PR) compar
    … 






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News – Macular Edema: The search for the cure continues

Can any other treatment beat anti-VEGF in macular edema?

(Note: companies that could be impacted by the content of this article are listed at the base of the story (desktop version). This article uses third-party references to provide a bullish, bearish and balanced point of view; sources listed in the “Balanced” section)

Macular edema (ME) is an eye disease condition that causes the sudden or chronic decrease in visual acuity. The condition arises from fluid accumulation within the macula, an area in the center of the retina, leading to vascular instability and the breakdown of the blood-retinal barrier (BRB). Characterization of the diseases is made by the swelling and thickening of the macula distorting a person’s central vision, causing a decline in visual acuity and eventually could lead to blindness.

Major causes of macular edema include diabetes, branch and central retinal vein occlusion, choroidal neovascularization, posterior uveitis, postoperative inflammation and central serous chorioretinopathy.

Fluid accumulation results from an imbalance between processes governing fluid entry and exit, when inner or outer blood-retinal barriers are disrupted. ME can arise from various conditions:

  1. 7 million subjects due to diabetes, called diabetic macular edema (DME)
  2. 3 million subjects due to vein occlusion
  3. 40% of visual impairment in patients with uveitis
  4. 5% of individuals older than 60 years of age due to neovascular age-related macular degeneration (AMD) in industrialized countries

ME treatment is a rapidly growing market with an increasing elderly population, and people living with diabetes. The anti-vascular endothelial growth factor (VEGF) therapy has revolutionized the treatment landscape for ME providing benefit to patients, however 30-50% of patients don’t respond or develop resistance to anti-VEGF treatment and the opportunity still remains for the development of novel compounds.

Research – TherapeuticsMD (TXMD) — Assumption of Coverage

Monday, April 1, 2019

TherapeuticsMD (TXMD)

.

TherapeuticsMD Inc is a major drug manufacturing with a focus on creating and commercializing products targeted exclusively for women. The company intends to commercialize advanced hormone therapy pharmaceutical products. TherapeuticsMD’s drug candidates that have completed clinical trials are designed to alleviate the symptoms of and reduce the health risks resulting from menopause-related hormone deficiencies, including hot flashes, osteoporosis, and discomfort. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating. 







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A Video Introduction to Enochian Biosciences


Enochian Biosciences Inc. is a biopharmaceutical levering its gene therapy platform to treat patients with HIV/AIDS. The company has a diverse pipeline at the preclinical and discovery stage to treat and prevent infectious disease and cancer. In the infectious disease front, there are two key products i) the lead candidate, genetically modified cell therapy ENO-1001, that is currently at preclinical stage for treatment of patients with HIV/AIDS and ii) ENO-2001, a vaccine, to prevent HIV infection. In the oncology front, Enochian is developing agents ENO-1002, ENO-3001, and ENO-5001 to treat patients with relapse metastatic colon cancer. The company has established research and development agreements with Scripps Research Institute to conduct pre-new drug application (pre-IND) work to advance ENO-1001 in the clinic, and with University of California Los Angles (UCLA) to advance HIV program. Enochian BioSciences is headquartered in Los Angeles, California.

Link to Enochian page on Channelchek

Podcast Launch: The Science of Investing in Biotechs

First Episode: The science of investing in biotechs

In the inaugural episode, Brant Pinvidic (host of the iTunes top-trending Hollywood podcast “Why I’m Not…”) tries to navigate the minefield of challenges that biotech investors face. In his engaging everyman approach, Brant looks at the importance of getting a third-party, independent opinion, how to determine what’s real and unreal about patent protection and intellectual property, and probes into where you might find the next breakthrough in medicine. He’s not alone on this challenge. Joined by four of the members of the Noble Scientific Advisory Board – the who’s who of life sciences – together they show you how a detailed and disciplined approach, in this risk-reward-rich field, is the true science behind investing in biotechs.

Who should listen? Anyone who wants to invest in life science companies but may be afraid; EVERY CEO and CFO of a biotech company, as this elite group will be sure to provide some eye-openers; investment professionals who can help advise their clients in what to look for… and what to avoid when trying to sift through the hundreds and hundreds of life sciences companies, and find that gem to invest in, and; anyone interested in a lively debate among some of the world’s greatest minds in medicine…

The most innovative Ideas, the inspirational People behind them, and the wealth of Opportunities they create… that’s IPO from Channelchek.

watch the IPO series trailer

Research – Dyadic (DYAI) – 2018 full year update

Thursday, March 28, 2019

Dyadic International (DYAI)

Could 2019 be transformational?

Dyadic International Inc. is a biotechnology company developing a proprietary expression platform to manufacture of biologic products. The company is employing C1 technology, part of a fungi expression system, to produce variety of modalities of biologic products, including vaccines, oncolytic viruses, monoclonal and bispecific antibodies, as well as biosimilars. 

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.  

  • R&D
    Advancement. 
    The company continues to make progression in
    establishing C1 expression production and the purification process in multiple
    projects. The Schmallenberg virus (SBV) as part of the ZAPI project exceeded
    the intended expression levels (17x), and is potentially the first to enter in
    human trials. We believe glycan engineering intended in 2019 could be
    transformational for the company.
  • Corporate
    Updates. 
    The proof of concept collaborations totaled nine projects,
    including two newly added agreements with large pharmaceuticals in Q1 2019.
    Dyadic continues to validate C1’s potential in biologic manufacturing, guiding
    an $8-$10 million burn rate this year. However, business development efforts
    are ongo
    … 







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